The roles of nuclear orphan receptor NR2F6 in anti-viral innate immunity.
Chen YangChen-Yu WangQiao-Yun LongZhuo CaoMing-Liang WeiShan-Bo TangXiang LinZi-Qi MuYong XiaoMing-Kai ChenMin WuLian-Yun LiPublished in: PLoS pathogens (2024)
Proper transcription regulation by key transcription factors, such as IRF3, is critical for anti-viral defense. Dynamics of enhancer activity play important roles in many biological processes, and epigenomic analysis is used to determine the involved enhancers and transcription factors. To determine new transcription factors in anti-DNA-virus response, we have performed H3K27ac ChIP-Seq and identified three transcription factors, NR2F6, MEF2D and MAFF, in promoting HSV-1 replication. NR2F6 promotes HSV-1 replication and gene expression in vitro and in vivo, but not dependent on cGAS/STING pathway. NR2F6 binds to the promoter of MAP3K5 and activates AP-1/c-Jun pathway, which is critical for DNA virus replication. On the other hand, NR2F6 is transcriptionally repressed by c-Jun and forms a negative feedback loop. Meanwhile, cGAS/STING innate immunity signaling represses NR2F6 through STAT3. Taken together, we have identified new transcription factors and revealed the underlying mechanisms involved in the network between DNA viruses and host cells.
Keyphrases
- transcription factor
- gene expression
- dna binding
- circulating tumor
- cell free
- single molecule
- sars cov
- genome wide identification
- induced apoptosis
- dna methylation
- single cell
- dendritic cells
- cell proliferation
- nucleic acid
- circulating tumor cells
- high throughput
- binding protein
- cell death
- endoplasmic reticulum stress
- network analysis